Quality of life in caregivers of a child with a developmental and epileptic encephalopathy.
Eden G RobertsonLauren KeladaStephanie BestIlias GoranitisKristine Piercenull nullAnnie ByeEmma Elizabeth PalmerPublished in: Developmental medicine and child neurology (2023)
Future research should explore whether interventions that help caregivers cognitively reframe the negative experiences of having a child with a DEE, and support them to partake in activities they enjoy, boost their SCrQoL.